safePICO70 956-608Recalls & reported problems
Radiometer Medical ApS · safePICO70 22Gx32mm Arterial blood sampler with 22Gx32mm needle, with neddle shield device (nsd), 1.5 mL, box of 100 pcs. · Class 2
All models of safePICO70 (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05700699566089), received between Nov 19, 2025 and Nov 19, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Corroded” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Corroded1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2025Corroded; Corroded
RADIOMETER REFERENCE NUMBER: (B)(4). ACCORDING TO COMPLAINT, THE CUSTOMER REPORTED MULTIPLE SAFEPICO70 SAMPLERS (TOTAL OF 4 SAMPLERS FOR LOT NUMBER DU50 AND A TOTAL OF 9 SAMPLERS FOR LOT NUMBER DX51) EXHIBITING SIGNS OF CORROSION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23593262 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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